Total synthesis of (+)-sundiversifolide.

Total synthesis of (+)-sundiversifolide.
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DOI:
10.1021/ol062960h
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发表时间:
2007-02
期刊:
影响因子:
5.2
通讯作者:
Hiromasa Yokoe;Hiroyuki Sasaki;T. Yoshimura;M. Shindo;Masahiro Yoshida;K. Shishido
Hiromasa Yokoe;Hiroyuki Sasaki;T. Yoshimura;M. Shindo;Masahiro Yoshida;K. Shishido
中科院分区:
化学1区
文献类型:
--
作者:
Hiromasa Yokoe;Hiroyuki Sasaki;T. Yoshimura;M. Shindo;Masahiro Yoshida;K. Shishido

文献摘要

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第一,对映体控制的全合成(+)-sundiverifolide已完成使用顺序的闭环复分解,[3,3]-sigmatropic重排,碘内酯化的顺式稠合氧杂双环[5.3.0]癸烯框架的天然产物的关键组件。[结构:见正文]
The first, enantiocontrolled total synthesis of (+)-sundiversifolide has been accomplished using the sequential ring-closing metathesis, [3,3]-sigmatropic rearrangement, and iodolactonization for the key assembly of the cis-fused oxabicyclo[5.3.0]decene framework of the natural product. [structure: see text]